# Potassium Chloride

NDC: 0121-1896
Generic name: POTASSIUM CHLORIDE
Labeler / Manufacturer: PAI Holdings, LLC dba PAI Pharma
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20230327

FDA application: ANDA210766

## Active ingredients

- POTASSIUM CHLORIDE: 20 meq/30mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0121-1896"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0121-1896
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e848477f-b10d-4249-b322-b70cd6a062de